Convenient and Universal Fabrication Method for Antibody–Enzyme Complexes as Sensing Elements Using the SpyCatcher/SpyTag System

Antibody–enzyme complexes (AECs) are ideal sensing elements, especially when oxidoreductases are used as the enzymes in the complex, with the potential to carry out rapid electrochemical measurements. However, conventional methods for the fabrication of AECs, including direct fusion and chemical con...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Analytical chemistry (Washington) 2018-12, Vol.90 (24), p.14500-14506
Hauptverfasser: Kimura, Hayato, Asano, Ryutaro, Tsukamoto, Natsumi, Tsugawa, Wakako, Sode, Koji
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 14506
container_issue 24
container_start_page 14500
container_title Analytical chemistry (Washington)
container_volume 90
creator Kimura, Hayato
Asano, Ryutaro
Tsukamoto, Natsumi
Tsugawa, Wakako
Sode, Koji
description Antibody–enzyme complexes (AECs) are ideal sensing elements, especially when oxidoreductases are used as the enzymes in the complex, with the potential to carry out rapid electrochemical measurements. However, conventional methods for the fabrication of AECs, including direct fusion and chemical conjugation, are associated with issues regarding the generation of insoluble aggregates and production of homogeneous AECs. Here, we developed a convenient and universal method for the fabrication of homogeneous AECs using the SpyCatcher/SpyTag system. We used an anti-epidermal growth factor receptor (EGFR) variable domain of a heavy chain antibody (VHH) and a glucose dehydrogenase (GDH) derived from Aspergillus flavus (AfGDH) as the model antibody and enzyme, respectively. Both SpyTag-fused VHH and SpyCatcher-fused AfGDH were successfully prepared using an Escherichia coli expression system, whereas anti-EGFR AECs were produced by simply mixing the two fusion proteins. A bivalent AEC, AfGDH with two VHH at both terminals, was also prepared and exhibited an increased affinity. A soluble EGFR was successfully detected in a dose-dependent manner using immobilized anti-EGFR immunoglobulin G (IgG) and bivalent AEC. We also confirmed the universality of this AEC fabricating method by applying it to another VHH. This method results in the convenient and universal preparation of sensing elements with the potential for electrochemical measurement.
doi_str_mv 10.1021/acs.analchem.8b04344
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2133434965</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2133434965</sourcerecordid><originalsourceid>FETCH-LOGICAL-a488t-ceb11bb7abd30c6bb8cb144e5d7be4ee0fd6cc974f4d933e9da1b01e03bd143</originalsourceid><addsrcrecordid>eNp9kctOGzEUhq2qqKS0b1BVlrrpZsLx2JnLEo1CqUTVRWA98uUMGTRjp7aDmK4Qr9A35EnqNIEFi65sS9__--h8hHxiMGeQs1Opw1xaOeg1jvNKgeBCvCEztsghK6oqf0tmAMCzvAQ4Ju9DuAVgDFjxjhxzEHnJSpiRx8bZO7Q92kilNfTa9nfogxzouVS-1zL2ztIfGNfO0M55emZjr5yZnh7-LO3vaUTauHEz4D0GKgNdoQ29vaHLAcfUGej1v2dcI11tpkbGNK4_TdcreUNXU4g4fiBHnRwCfjycJ2R1vrxqLrLLn9--N2eXmRRVFTONijGlSqkMB10oVWnFhMCFKRUKROhMoXVdik6YmnOsjWQKGAJXhgl-Qr7uWzfe_dpiiO3YB43DIC26bWhzxnlaYV0sEvrlFXrrtj6tekcVYpHXjFWJEntKexeCx67d-H6UfmoZtDtDbTLUPhtqD4ZS7POhfKtGNC-hZyUJgD2wi798_N_OvxRxo7Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2164529118</pqid></control><display><type>article</type><title>Convenient and Universal Fabrication Method for Antibody–Enzyme Complexes as Sensing Elements Using the SpyCatcher/SpyTag System</title><source>ACS Publications</source><creator>Kimura, Hayato ; Asano, Ryutaro ; Tsukamoto, Natsumi ; Tsugawa, Wakako ; Sode, Koji</creator><creatorcontrib>Kimura, Hayato ; Asano, Ryutaro ; Tsukamoto, Natsumi ; Tsugawa, Wakako ; Sode, Koji</creatorcontrib><description>Antibody–enzyme complexes (AECs) are ideal sensing elements, especially when oxidoreductases are used as the enzymes in the complex, with the potential to carry out rapid electrochemical measurements. However, conventional methods for the fabrication of AECs, including direct fusion and chemical conjugation, are associated with issues regarding the generation of insoluble aggregates and production of homogeneous AECs. Here, we developed a convenient and universal method for the fabrication of homogeneous AECs using the SpyCatcher/SpyTag system. We used an anti-epidermal growth factor receptor (EGFR) variable domain of a heavy chain antibody (VHH) and a glucose dehydrogenase (GDH) derived from Aspergillus flavus (AfGDH) as the model antibody and enzyme, respectively. Both SpyTag-fused VHH and SpyCatcher-fused AfGDH were successfully prepared using an Escherichia coli expression system, whereas anti-EGFR AECs were produced by simply mixing the two fusion proteins. A bivalent AEC, AfGDH with two VHH at both terminals, was also prepared and exhibited an increased affinity. A soluble EGFR was successfully detected in a dose-dependent manner using immobilized anti-EGFR immunoglobulin G (IgG) and bivalent AEC. We also confirmed the universality of this AEC fabricating method by applying it to another VHH. This method results in the convenient and universal preparation of sensing elements with the potential for electrochemical measurement.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/acs.analchem.8b04344</identifier><identifier>PMID: 30427170</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Bacterial proteins ; Chemistry ; Conjugation ; Detection ; E coli ; Electrochemistry ; Enzymes ; Epidermal growth factor ; Epidermal growth factor receptors ; Fabrication ; Glucose dehydrogenase ; Growth factors ; Immunoglobulin G ; Immunoglobulins ; Measurement methods ; Organic chemistry ; Proteins</subject><ispartof>Analytical chemistry (Washington), 2018-12, Vol.90 (24), p.14500-14506</ispartof><rights>Copyright American Chemical Society Dec 18, 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a488t-ceb11bb7abd30c6bb8cb144e5d7be4ee0fd6cc974f4d933e9da1b01e03bd143</citedby><cites>FETCH-LOGICAL-a488t-ceb11bb7abd30c6bb8cb144e5d7be4ee0fd6cc974f4d933e9da1b01e03bd143</cites><orcidid>0000-0001-6795-8377</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.analchem.8b04344$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.analchem.8b04344$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30427170$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kimura, Hayato</creatorcontrib><creatorcontrib>Asano, Ryutaro</creatorcontrib><creatorcontrib>Tsukamoto, Natsumi</creatorcontrib><creatorcontrib>Tsugawa, Wakako</creatorcontrib><creatorcontrib>Sode, Koji</creatorcontrib><title>Convenient and Universal Fabrication Method for Antibody–Enzyme Complexes as Sensing Elements Using the SpyCatcher/SpyTag System</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. Chem</addtitle><description>Antibody–enzyme complexes (AECs) are ideal sensing elements, especially when oxidoreductases are used as the enzymes in the complex, with the potential to carry out rapid electrochemical measurements. However, conventional methods for the fabrication of AECs, including direct fusion and chemical conjugation, are associated with issues regarding the generation of insoluble aggregates and production of homogeneous AECs. Here, we developed a convenient and universal method for the fabrication of homogeneous AECs using the SpyCatcher/SpyTag system. We used an anti-epidermal growth factor receptor (EGFR) variable domain of a heavy chain antibody (VHH) and a glucose dehydrogenase (GDH) derived from Aspergillus flavus (AfGDH) as the model antibody and enzyme, respectively. Both SpyTag-fused VHH and SpyCatcher-fused AfGDH were successfully prepared using an Escherichia coli expression system, whereas anti-EGFR AECs were produced by simply mixing the two fusion proteins. A bivalent AEC, AfGDH with two VHH at both terminals, was also prepared and exhibited an increased affinity. A soluble EGFR was successfully detected in a dose-dependent manner using immobilized anti-EGFR immunoglobulin G (IgG) and bivalent AEC. We also confirmed the universality of this AEC fabricating method by applying it to another VHH. This method results in the convenient and universal preparation of sensing elements with the potential for electrochemical measurement.</description><subject>Bacterial proteins</subject><subject>Chemistry</subject><subject>Conjugation</subject><subject>Detection</subject><subject>E coli</subject><subject>Electrochemistry</subject><subject>Enzymes</subject><subject>Epidermal growth factor</subject><subject>Epidermal growth factor receptors</subject><subject>Fabrication</subject><subject>Glucose dehydrogenase</subject><subject>Growth factors</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulins</subject><subject>Measurement methods</subject><subject>Organic chemistry</subject><subject>Proteins</subject><issn>0003-2700</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kctOGzEUhq2qqKS0b1BVlrrpZsLx2JnLEo1CqUTVRWA98uUMGTRjp7aDmK4Qr9A35EnqNIEFi65sS9__--h8hHxiMGeQs1Opw1xaOeg1jvNKgeBCvCEztsghK6oqf0tmAMCzvAQ4Ju9DuAVgDFjxjhxzEHnJSpiRx8bZO7Q92kilNfTa9nfogxzouVS-1zL2ztIfGNfO0M55emZjr5yZnh7-LO3vaUTauHEz4D0GKgNdoQ29vaHLAcfUGej1v2dcI11tpkbGNK4_TdcreUNXU4g4fiBHnRwCfjycJ2R1vrxqLrLLn9--N2eXmRRVFTONijGlSqkMB10oVWnFhMCFKRUKROhMoXVdik6YmnOsjWQKGAJXhgl-Qr7uWzfe_dpiiO3YB43DIC26bWhzxnlaYV0sEvrlFXrrtj6tekcVYpHXjFWJEntKexeCx67d-H6UfmoZtDtDbTLUPhtqD4ZS7POhfKtGNC-hZyUJgD2wi798_N_OvxRxo7Q</recordid><startdate>20181218</startdate><enddate>20181218</enddate><creator>Kimura, Hayato</creator><creator>Asano, Ryutaro</creator><creator>Tsukamoto, Natsumi</creator><creator>Tsugawa, Wakako</creator><creator>Sode, Koji</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6795-8377</orcidid></search><sort><creationdate>20181218</creationdate><title>Convenient and Universal Fabrication Method for Antibody–Enzyme Complexes as Sensing Elements Using the SpyCatcher/SpyTag System</title><author>Kimura, Hayato ; Asano, Ryutaro ; Tsukamoto, Natsumi ; Tsugawa, Wakako ; Sode, Koji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a488t-ceb11bb7abd30c6bb8cb144e5d7be4ee0fd6cc974f4d933e9da1b01e03bd143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Bacterial proteins</topic><topic>Chemistry</topic><topic>Conjugation</topic><topic>Detection</topic><topic>E coli</topic><topic>Electrochemistry</topic><topic>Enzymes</topic><topic>Epidermal growth factor</topic><topic>Epidermal growth factor receptors</topic><topic>Fabrication</topic><topic>Glucose dehydrogenase</topic><topic>Growth factors</topic><topic>Immunoglobulin G</topic><topic>Immunoglobulins</topic><topic>Measurement methods</topic><topic>Organic chemistry</topic><topic>Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kimura, Hayato</creatorcontrib><creatorcontrib>Asano, Ryutaro</creatorcontrib><creatorcontrib>Tsukamoto, Natsumi</creatorcontrib><creatorcontrib>Tsugawa, Wakako</creatorcontrib><creatorcontrib>Sode, Koji</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts – Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical chemistry (Washington)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kimura, Hayato</au><au>Asano, Ryutaro</au><au>Tsukamoto, Natsumi</au><au>Tsugawa, Wakako</au><au>Sode, Koji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Convenient and Universal Fabrication Method for Antibody–Enzyme Complexes as Sensing Elements Using the SpyCatcher/SpyTag System</atitle><jtitle>Analytical chemistry (Washington)</jtitle><addtitle>Anal. Chem</addtitle><date>2018-12-18</date><risdate>2018</risdate><volume>90</volume><issue>24</issue><spage>14500</spage><epage>14506</epage><pages>14500-14506</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><abstract>Antibody–enzyme complexes (AECs) are ideal sensing elements, especially when oxidoreductases are used as the enzymes in the complex, with the potential to carry out rapid electrochemical measurements. However, conventional methods for the fabrication of AECs, including direct fusion and chemical conjugation, are associated with issues regarding the generation of insoluble aggregates and production of homogeneous AECs. Here, we developed a convenient and universal method for the fabrication of homogeneous AECs using the SpyCatcher/SpyTag system. We used an anti-epidermal growth factor receptor (EGFR) variable domain of a heavy chain antibody (VHH) and a glucose dehydrogenase (GDH) derived from Aspergillus flavus (AfGDH) as the model antibody and enzyme, respectively. Both SpyTag-fused VHH and SpyCatcher-fused AfGDH were successfully prepared using an Escherichia coli expression system, whereas anti-EGFR AECs were produced by simply mixing the two fusion proteins. A bivalent AEC, AfGDH with two VHH at both terminals, was also prepared and exhibited an increased affinity. A soluble EGFR was successfully detected in a dose-dependent manner using immobilized anti-EGFR immunoglobulin G (IgG) and bivalent AEC. We also confirmed the universality of this AEC fabricating method by applying it to another VHH. This method results in the convenient and universal preparation of sensing elements with the potential for electrochemical measurement.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>30427170</pmid><doi>10.1021/acs.analchem.8b04344</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-6795-8377</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0003-2700
ispartof Analytical chemistry (Washington), 2018-12, Vol.90 (24), p.14500-14506
issn 0003-2700
1520-6882
language eng
recordid cdi_proquest_miscellaneous_2133434965
source ACS Publications
subjects Bacterial proteins
Chemistry
Conjugation
Detection
E coli
Electrochemistry
Enzymes
Epidermal growth factor
Epidermal growth factor receptors
Fabrication
Glucose dehydrogenase
Growth factors
Immunoglobulin G
Immunoglobulins
Measurement methods
Organic chemistry
Proteins
title Convenient and Universal Fabrication Method for Antibody–Enzyme Complexes as Sensing Elements Using the SpyCatcher/SpyTag System
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T12%3A50%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Convenient%20and%20Universal%20Fabrication%20Method%20for%20Antibody%E2%80%93Enzyme%20Complexes%20as%20Sensing%20Elements%20Using%20the%20SpyCatcher/SpyTag%20System&rft.jtitle=Analytical%20chemistry%20(Washington)&rft.au=Kimura,%20Hayato&rft.date=2018-12-18&rft.volume=90&rft.issue=24&rft.spage=14500&rft.epage=14506&rft.pages=14500-14506&rft.issn=0003-2700&rft.eissn=1520-6882&rft_id=info:doi/10.1021/acs.analchem.8b04344&rft_dat=%3Cproquest_cross%3E2133434965%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2164529118&rft_id=info:pmid/30427170&rfr_iscdi=true